1196-17-4 Usage
Uses
Used in Flavoring and Fragrance Industry:
2,3-dihydro-1H-inden-1-ylmethanol is used as a flavoring agent in food and beverages, adding a sweet, spicy taste to various products. It is also used in the fragrance industry to create unique scents for perfumes and other scented products.
Used in Cosmetic Industry:
In the cosmetic industry, 2,3-dihydro-1H-inden-1-ylmethanol is used as a key ingredient in various formulations, providing a pleasant scent and enhancing the sensory experience of cosmetic products.
Used in Pharmaceutical Synthesis:
2,3-dihydro-1H-inden-1-ylmethanol is used as a starting material in the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Antioxidant Applications:
Due to its antioxidant properties, 2,3-dihydro-1H-inden-1-ylmethanol is used in various applications to protect against oxidative stress and prevent the formation of harmful free radicals.
Used in Anti-inflammatory Applications:
Leveraging its anti-inflammatory properties, 2,3-dihydro-1H-inden-1-ylmethanol is used in formulations to reduce inflammation and alleviate pain associated with various conditions.
Used in Antimicrobial Applications:
2,3-dihydro-1H-inden-1-ylmethanol is used as an antimicrobial agent in various applications, including food preservation, cosmetics, and pharmaceuticals, to inhibit the growth of harmful microorganisms and maintain product safety and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 1196-17-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1196-17:
(6*1)+(5*1)+(4*9)+(3*6)+(2*1)+(1*7)=74
74 % 10 = 4
So 1196-17-4 is a valid CAS Registry Number.
1196-17-4Relevant academic research and scientific papers
Acid-Promoted Hydroformylative Synthesis of Alcohol with Carbon Dioxide by Heterobimetallic Ruthenium-Cobalt Catalytic System
Zhang, Xuehua,Tian, Xinxin,Shen, Chaoren,Xia, Chungu,He, Lin
, p. 1986 - 1992 (2019/03/17)
The acid-aided heterobimetallic ruthenium-cobalt catalytic system for the reductive hydroformylation with carbon dioxide was established. Various alkenes, including waste from biomass and petroleum industry, could be upgraded to valuable alcohols with this protocol. Acid-promoted reverse water-gas shift (RWGS), thereby accelerating the hydroformylative synthesis of alcohol. The theoretical computations revealed that acid promoted RWGS by facilitating the dehydroxylation of ruthenium hydroxy carbonyl intermediate.
Metal-free synthesis of indanes by iodine(iii)-mediated ring contraction of 1,2-dihydronaphthalenes
Siqueira, Fernanda A.,Ishikawa, Eloisa E.,Fogac?a, Andre?,Faccio, Andre?a T.,Carneiro, Va?nia M. T.,Soares, Rafael R. S.,Utaka, Aline,Te?be?ka, Iris R. M.,Bielawski, Marcin,Olofsson, Berit,Silva Jr., Luiz F.
experimental part, p. 1795 - 1807 (2012/06/01)
A metal-free protocol was developed to synthesize indanes by ring contraction of 1,2-dihydronaphthalenes promoted by PhI(OH)OTs (HTIB or Koser's reagent). This oxidative rearrangement can be performed in several solvents (MeOH, CH3CN, 2,2,2-trifluoroethanol (TFE), 1,1,1,3,3,3-hexafluoroisopropanol (HFIP), and a 1:4 mixture of TFE:CH2Cl2) under mild conditions. The ring contraction diastereoselectively gives functionalized trans-1,3-disubstituted indanes, which are difficult to obtain in synthetic organic chemistry. ?2011 Sociedade Brasileira de Qui?mica.
